An exciting Medical Device Manufacturing company is looking to bring a Senior Manager of Regulatory Affairs to their growing team. They are looking for highly motivated candidates with strong leadership experience.
The Senior Manger Regulatory Affairs will be responsible for:
- Managing a team of Regulatory professionals, while working cross-functionally with relevant departments
- Overseeing and collaborating in 510k and similar international submissions
- Providing oversight in internal and external audits
The Senior Manager Regulatory Affairs should have the following qualifications:
- 8 years of experience in the medical device field
- At least 5 years working in a management role
- Hands on experience working on 510k submissions for IVD
*Relocation assistance will be provided for qualified candidates
If you are interested in this position, please apply here
